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Control of Pancreatic β Cell Regeneration by Glucose Metabolism
Shay Porat, Noa Weinberg-Corem, Sharona Tornovsky-Babaey, Rachel Schyr-Ben-Haroush, Ayat Hija, Miri Stolovich-Rain, Daniela Dadon, Zvi Granot, Vered Ben-Hur, Peter White, Christophe A. Girard, Rotem Karni, Klaus H. Kaestner, Frances M. Ashcroft, Mark A. Magnuson, Ann Saada, Joseph Grimsby, Benjamin Glaser, Yuval Dor Cell Metabolism Volume 13, Issue 4, Pages (April 2011) DOI: /j.cmet Copyright © 2011 Elsevier Inc. Terms and Conditions
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Cell Metabolism 2011 13, 440-449DOI: (10.1016/j.cmet.2011.02.012)
Copyright © 2011 Elsevier Inc. Terms and Conditions
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Figure 1 Islet Transplantation Shows Systemic Regulation of Compensatory and Basal β Cell Replication and a Positive Effect of Glucose (A) βDTA mice grafted with wild-type islets. Top, schematic of experiment (left) and expected blood glucose levels after the addition of doxycycline and β cell ablation (right). Circles, native pancreas; ovals, transplanted islets; blue, wild-type; red, βDTA. Bottom, β cell replication in the pancreas (left) and in grafts (right). Table under graph provides estimated numbers of islets per mouse. Error bars represent standard error. (B) Wild-type mice engrafted with wild-type and βDTA islets. Top, schematic of experiment. Bottom, β cell replication in the pancreas (left) and in grafts (right). Table under graph provides estimated numbers of islets per mouse. Error bars represent standard error. (C) Wild-type mice engrafted with βKir islets (yellow before tamoxifen-induced expression, red after tamoxifen). Left, schematic of experiment. Right, β cell replication in the pancreas. Error bars represent standard error. Cell Metabolism , DOI: ( /j.cmet ) Copyright © 2011 Elsevier Inc. Terms and Conditions
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Figure 2 Relationship between Blood Glucose and β Cell Replication Rate (A) β cell replication rate as a function of blood glucose levels at sacrifice. Open symbols, wild-type mice; closed symbols, βDTA mice. Note a positive effect of glucose on replication rate, but no relationship between glucose levels and β cell replication rate within the transgenic group. (B) Proposed model for the effect of glucose, via workload of β cells, on β cell replication rate. The model explains how different normoglycemic conditions may cause different β cell replication rates. Cell Metabolism , DOI: ( /j.cmet ) Copyright © 2011 Elsevier Inc. Terms and Conditions
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Figure 3 Deletion of Glucokinase in Adult β Cells Reduces β Cell Replication Rate (A) Blood glucose (left) and serum insulin levels (right) 9 days after tamoxifen injection of insulin-CreER; GCKlox/lox mice (βGCK, red) or GCKlox/lox controls (blue). Measurements were taken in the fed state. Error bars represent standard error. (B) Increased phosphorylation of AMPK in βGCK islets, 9 days after tamoxifen injection, providing evidence for low intracellular energy charge despite high blood glucose levels. Original magnification, 800×. (C) Reduced β cell replication rate in βGCK islets, 9 days after tamoxifen injection. Error bars represent standard error. Cell Metabolism , DOI: ( /j.cmet ) Copyright © 2011 Elsevier Inc. Terms and Conditions
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Figure 4 Effects of Glucokinase Activator on β Cells In Vivo
(A) Reduced blood glucose levels following a single oral administration of GKA (50 mg/kg) or vehicle (DMSO) to wild-type mice. n > 10 mice in each group. Error bars represent standard error. (B) Increased glucose oxidation in wild-type islets exposed to GKA at different glucose levels. Error bars represent standard error. (C) Increased β cell replication, measured as fraction of Ki67+ β cells, 17 hr after administration of GKA or vehicle (DMSO) to 6-week-old wild-type mice. n refers to number of mice analyzed; for each mouse, >2000 β cells were counted. Error bars represent standard error. (D) Increased incorporation of BrdU in β cells of mice treated with a single dose of GKA. Error bars represent standard error. (E) GKA-induced β cell replication is abolished in mice deficient for GCK in β cells (green and black bars). NS, not significant. n = number of mice analyzed. Error bars represent standard error. (F) GKA moderately increases the fraction of replicating β cells in hyperglycemic βDTA mice. Error bars represent standard error. Cell Metabolism , DOI: ( /j.cmet ) Copyright © 2011 Elsevier Inc. Terms and Conditions
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Figure 5 Dependence of β Cell Replication Downstream of Glucokinase on Membrane Depolarization (A) Left, effect of diazoxide (40 mg/kg) on blood glucose levels from injection to sacrifice 24 hr later. Right, diazoxide abolishes GKA-induced β cell replication in wild-type mice. n = number of mice analyzed. Error bars represent standard error. (B) Left, effect of transgenic expression of Kir6.2 V59M in adult β cells (βKir) on blood glucose levels. Right, the Kir6.2 mutation reduces basal β cell replication and abolishes GKA-induced β cell replication. Tamoxifen was injected on day 0 to activate the mutant gene. GKA and vehicle were administered on day 2. Error bars represent standard error. (C) Left, blood glucose levels in βGCK mutants and GCKlox/lox littermate controls in response to glyburide. Right, acute rescue of β cell replication in βGCK mutants by glyburide (Glyb). Glyburide was given by oral gavage at 20 mg/kg. Error bars represent standard error. (D) Left, effect of glyburide on blood glucose in diabetic βDTA mice. Right, glyburide increases the fraction of Ki67+ β cells in diabetic βDTA mice. Error bars represent standard error. Cell Metabolism , DOI: ( /j.cmet ) Copyright © 2011 Elsevier Inc. Terms and Conditions
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